A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673667



Internal ID15410319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:131013557..131381745hg38UCSC Ensembl
Innerchr12:131498102..131866290hg19UCSC Ensembl
Innerchr12:130064055..130432243hg18UCSC Ensembl
Innerchr12:130022982..130391170hg17UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38368189
hg19368189
hg18368189
hg17368189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517271
Supporting Variants
Samples
Known GenesGPR133, LOC116437, LOC338797
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673667
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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